FDA Adverse Event Malfunction Summary report: N

TRANSPORT SERIES

MDR report key: 2070447 · Received March 29, 2011

Report

Report Number
1831750-2011-03027
Event Type
Malfunction
Date Received
March 29, 2011
Date of Event
March 1, 2011
Report Date
March 1, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

EVAL: PLUNGER.

Description of Event or Problem · 1

IT WAS REPORTED BY SVC REPORT THAT THERE WAS A BAD GAS CYLINDER AND THE FOWLER COULD NOT BE RAISED OR LOWERED COMPLETELY. IT IS UNK IF THERE WAS PT INVOLVEMENT OR ADVERSE CONSEQUENCES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRANSPORT SERIES HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0721 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK